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Elongation method at restricted open-shell Hartree–Fock level of theory

Authors

  • Jacek Korchowiec,

    Corresponding author
    1. K. Gumiński Department of Theoretical Chemistry, Jagiellonian University, R. Ingardena 3, 30-060 Cracow, Poland
    2. Group, PRESTO, Japan Science and Technology Agency (JST), Kawaguchi Center Building, Honcho 4-1-8, Kawaguchi, Saitama, 332-0012, Japan
    • K. Gumiński Department of Theoretical Chemistry, Jagiellonian University, R. Ingardena 3, 30-060 Cracow, Poland
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  • Feng Long Gu,

    1. Department of Molecular and Material Sciences, Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasuga-Park, Fukuoka, 816-8580, Japan
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  • Yuriko Aoki

    1. Department of Molecular and Material Sciences, Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasuga-Park, Fukuoka, 816-8580, Japan
    2. Group, PRESTO, Japan Science and Technology Agency (JST), Kawaguchi Center Building, Honcho 4-1-8, Kawaguchi, Saitama, 332-0012, Japan
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Abstract

Elongation and cutoff elongation methods are described at the restricted open-shell Hartree–Fock (ROHF) level of theory. Test calculations are performed for polyethylene radicals CH3-(CH2)N−1 (N = 8, 10, 12, … 40), using minimal (STO-3G) and valence double-ζ (6-31G) basis sets. It is demonstrated that the process of diminishing the variational space in the elongation method does not introduce a large error, and that the error can be controlled by the size of the starting radical. Implementation of the cutoff technique to the elongation method leads to distinct time savings in the self-consistent field (SCF) process and does not worsen the results. In contrast to full variational space ROHF treatment, the step SCF CPU time in the cutoff elongation calculations appears to saturate to an asymptotic value that permits investigation of large molecular systems. © 2005 Wiley Periodicals, Inc. Int J Quantum Chem, 2005

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